Specialist I, Global Clinical Solutions

Job Title: Specialist, Global Clinical Solutions

Introduction to role:

Are you ready to turn meticulous clinical data practice into faster, smarter decisions that bring medicines to patients sooner? Do you thrive at the intersection of study delivery, data integrity and user support, where robust systems and precise coding enable teams to move with confidence?

As Specialist, Global Clinical Solutions, you will be a key partner to study teams, ensuring the clinical systems and coding foundations that keep global trials running at pace. You will connect day-to-day delivery with long-term improvement by safeguarding data quality, supporting users, and shaping non-drug project proposals that strengthen how we work. Your impact will be felt in the accuracy of our records, the clarity of our queries, and the speed at which we resolve issues—so our science can advance without friction.

You will collaborate across clinical development, data management and operations, maintaining high standards while sharing protocols that scale. Anchored in real-world study needs and driven by curiosity, you will help us push boundaries with rigor, attention to detail and a service attitude that enables teams worldwide.

Accountabilities:

• Case Support: Contribute to the development of arguments that prioritize non-drug project proposals, linking investment to measurable study delivery value.
• Study Support Systems Stewardship: Maintain systems associated with Financial Disclosure, Drug Return and Destruction, Pairs Investigator Database, Investigator Safety Letter Distribution and Clinical Trial Registration to standards of quality and consistency.
• First-Line User Support: Provide timely, appropriate user support for study delivery systems, resolving issues and guiding users to keep studies moving.
• Data Integrity and Financial Processing: Monitor data integrity in study delivery systems and process financial charges associated with study delivery support activities.
• Clinical Coding Excellence: Perform accurate, consistent hands-on coding or review of CRO-coded clinical study data (medical history, surgical history, adverse events, drugs) using agreed versions of clinical coding dictionaries and guidelines.
• Query and Issue Management: Raise and resolve coding-related queries according to global and local processes and study timelines; monitor and respond to coding-related GDMRs from Clinical Development and advance to the GCDMT as required.
• Knowledge Sharing and Communication: Work with team members across the organization to share knowledge, experiences and protocols; develop and maintain communication tools that support study delivery.
• Integration and Continuous Improvement: Support business objectives and the global integration of systems and services, contributing ideas and actions that drive consistency and scalability.
• Safety, Health and Environment: Meet high SHE standards and legal obligations in all activities.
• Leadership and Culture: Demonstrate a willingness to take on project activities at any level consistent with experience, fostering courageous leadership, creativity and collaboration.

Essential Skills/Experience:

• Maintains systems associated with the Financial Disclosure, Drug Return and Destruction, Pairs Investigator Database, Investigator Safety Letter Distribution and Clinical Trial Registration to appropriate standards of quality and consistency.
• Provides appropriate 1st line user support and ensures monitoring of the integrity of data in the SD Systems as well as processing financial charges associated with Study Delivery Support activities.
• Performs accurate and consistent hands-on coding or review of CRO-coded Clinical Study data (e.g., medical history, surgical history, adverse events, drugs) using agreed versions of clinical coding dictionaries and appropriate guidelines, including raising queries, according to global and local processes, and study timelines.
• Monitors and responds to coding-related GDMRs submitted by Clinical Development and advances requests to the GCDMT according to established processes.
• Works with team and other members of the organization to share knowledge, experiences and protocols; develops and maintains communication tools supporting Study Delivery.
• Supports Study Delivery business objectives and global integration of systems and services.
• Meets high SHE standards and legal obligations.

Desirable Skills/Experience:

• Supports development of cases for prioritisation of non-drug project proposals.
• Demonstrates willingness to take on any level project activity consistent with current or past experience in support of study delivery.
• Has personal responsibility for creating a culture of courageous leadership, creativity and collaboration.

When we put unexpected teams in the same room, we ignite bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Why AstraZeneca:

Here, scientific curiosity meets practical delivery. You will partner with clinicians, data experts and operators who push boundaries with humility and purpose, backed by advanced digital, data science and AI capabilities that help us predict success and reduce risk. We learn fast, share openly and bring together diverse perspectives—from internal teams to collaborators in academia and industry—to solve hard problems and accelerate progress for patients. We value kindness alongside ambition, giving you the support to try new approaches and the freedom to improve how critical study systems and coding are done at global scale.

Call to Action:

If you are ready to turn meticulous system stewardship and clinical coding expertise into faster study decisions and real patient impact, step into this role and help shape how our trials run worldwide.

Date Posted

25-Feb-2026

Closing Date

03-Apr-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.